A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1876968



Internal ID17449791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18132374..18143365hg38UCSC Ensembl
Innerchr11:18153921..18164912hg19UCSC Ensembl
Innerchr11:18110497..18121488hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810992
hg1910992
hg1810992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971990
Supporting Variants
SamplesHGDP00778
Known GenesMRGPRX3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1876968
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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